Primary Site >> Stomach Cancer

Gene >> PPP2R1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111754539:111754539(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.989G>T
AA Mutation p.Arg330Ile(p.R330I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111742580:111742580(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1640A>T
AA Mutation p.Asn547Ile(p.N547I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111752197:111752197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1300G>A
AA Mutation p.Ala434Thr(p.A434T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111761009:111761009(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782083920
CDS Mutation c.349C>T
AA Mutation p.Arg117Cys(p.R117C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111752296:111752296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1201G>T
AA Mutation p.Asp401Tyr(p.D401Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111742118:111742118(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1724T>C
AA Mutation p.Val575Ala(p.V575A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000527614
Start 111754533:111754533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.995C>G
AA Mutation p.Thr332Ser(p.T332S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000527614
Start 111742107:111742107(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1735T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000311129
Start 111727016:111727016(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1953T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000527614
Start 111761028:111761028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.330T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000527614
Start 111759856:111759859(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.632_635delACAG
AA Mutation p.Asp211ValfsTer2(p.D211Vfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence splice_donor_variant
Transcription ID ENST00000527614
Start 111742052:111742052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1789+1G>T
Mutation Classification Splice_Site
Feature Type Transcript